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Journal Abstract Search

198 related items for PubMed ID: 10964557

  • 1. Caspase-8 specificity probed at subsite S(4): crystal structure of the caspase-8-Z-DEVD-cho complex.
    Blanchard H, Donepudi M, Tschopp M, Kodandapani L, Wu JC, Grütter MG.
    J Mol Biol; 2000 Sep 08; 302(1):9-16. PubMed ID: 10964557
    [Abstract] [Full Text] [Related]

  • 2. Structural and kinetic analysis of caspase-3 reveals role for s5 binding site in substrate recognition.
    Fang B, Boross PI, Tozser J, Weber IT.
    J Mol Biol; 2006 Jul 14; 360(3):654-66. PubMed ID: 16781734
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  • 3. Plasticity of S2-S4 specificity pockets of executioner caspase-7 revealed by structural and kinetic analysis.
    Agniswamy J, Fang B, Weber IT.
    FEBS J; 2007 Sep 14; 274(18):4752-65. PubMed ID: 17697120
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  • 4. Peptidyl beta-homo-aspartals (3-amino-4-carboxybutyraldehydes): new specific inhibitors of caspases.
    Bajusz S, Fauszt I, Németh K, Barabás E, Juhász A, Patthy M, Bauer PI.
    Biopolymers; 1999 Sep 14; 51(1):109-18. PubMed ID: 10380358
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  • 5. Homology modeling of nematode Caenorhabditis elegans CED3 protein-inhibitor complex.
    Azim MK, Grossmann JG, Zaidi ZH.
    Biochem Biophys Res Commun; 2001 Feb 16; 281(1):115-21. PubMed ID: 11178968
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  • 7. Exploring the S4 and S1 prime subsite specificities in caspase-3 with aza-peptide epoxide inhibitors.
    Ganesan R, Jelakovic S, Campbell AJ, Li ZZ, Asgian JL, Powers JC, Grütter MG.
    Biochemistry; 2006 Aug 01; 45(30):9059-67. PubMed ID: 16866351
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  • 9. Some commonly used caspase substrates and inhibitors lack the specificity required to monitor individual caspase activity.
    Pereira NA, Song Z.
    Biochem Biophys Res Commun; 2008 Dec 19; 377(3):873-7. PubMed ID: 18976637
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  • 11. Synthesis, enzymatic evaluation, and docking studies of fluorogenic caspase 8 tetrapeptide substrates.
    Reszka P, Schulz R, Methling K, Lalk M, Bednarski PJ.
    ChemMedChem; 2010 Jan 19; 5(1):103-17. PubMed ID: 19918833
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  • 12. Design, synthesis, and evaluation of aza-peptide Michael acceptors as selective and potent inhibitors of caspases-2, -3, -6, -7, -8, -9, and -10.
    Ekici OD, Li ZZ, Campbell AJ, James KE, Asgian JL, Mikolajczyk J, Salvesen GS, Ganesan R, Jelakovic S, Grütter MG, Powers JC.
    J Med Chem; 2006 Sep 21; 49(19):5728-49. PubMed ID: 16970398
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  • 13. Inhibition of apoptosis and clonogenic survival of cells expressing crmA variants: optimal caspase substrates are not necessarily optimal inhibitors.
    Ekert PG, Silke J, Vaux DL.
    EMBO J; 1999 Jan 15; 18(2):330-8. PubMed ID: 9889190
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  • 14. Identification of early intermediates of caspase activation using selective inhibitors and activity-based probes.
    Berger AB, Witte MD, Denault JB, Sadaghiani AM, Sexton KM, Salvesen GS, Bogyo M.
    Mol Cell; 2006 Aug 15; 23(4):509-21. PubMed ID: 16916639
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  • 17. LIGHT sensitizes IFN-gamma-mediated apoptosis of HT-29 human carcinoma cells through both death receptor and mitochondria pathways.
    Zhang MC, Liu HP, Demchik LL, Zhai YF, Yang DJ.
    Cell Res; 2004 Apr 15; 14(2):117-24. PubMed ID: 15115612
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  • 19. Differential protection with inhibitors of caspase-8 and caspase-3 in murine models of tumor necrosis factor and Fas receptor-mediated hepatocellular apoptosis.
    Bajt ML, Vonderfecht SL, Jaeschke H.
    Toxicol Appl Pharmacol; 2001 Sep 15; 175(3):243-52. PubMed ID: 11559023
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  • 20. X-ray structures of five renin inhibitors bound to saccharopepsin: exploration of active-site specificity.
    Cronin NB, Badasso MO, J Tickle I, Dreyer T, Hoover DJ, Rosati RL, Humblet CC, Lunney EA, Cooper JB.
    J Mol Biol; 2000 Nov 10; 303(5):745-60. PubMed ID: 11061973
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